| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 177001 | BAA02g18630 | A02 | 9547459 | G | A | upstream_gene_variant | MODIFIER | c.-4302C>T| |
S188 |
| 177002 | BAA02g18640 | A02 | 9548611 | G | A | upstream_gene_variant | MODIFIER | c.-2370C>T| |
S280 |
| 177003 | BAA02g18640 | A02 | 9548623 | C | T | upstream_gene_variant | MODIFIER | c.-2382G>A| |
S112 |
| 177004 | BAA02g18650 | A02 | 9548970 | G | A | missense_variant | MODERATE | c.95G>A|p.Arg32Lys |
S263 |
| 177005 | BAA02g18650 | A02 | 9549391 | G | A | synonymous_variant | LOW | c.270G>A|p.Leu90Leu |
S35 |
| 177006 | BAA02g18650 | A02 | 9549682 | C | T | synonymous_variant | LOW | c.421C>T|p.Leu141Leu |
S277 |
| 177007 | BAA02g18640 | A02 | 9549815 | G | A | upstream_gene_variant | MODIFIER | c.-3574C>T| |
S134 |
| 177008 | BAA02g18640 | A02 | 9550551 | G | A | upstream_gene_variant | MODIFIER | c.-4310C>T| |
S294 |
| 177009 | BAA02g18650 | A02 | 9552232 | C | T | downstream_gene_variant | MODIFIER | c.*2280C>T| |
S202 |
| 177010 | BAA02g18650 | A02 | 9553212 | G | A | downstream_gene_variant | MODIFIER | c.*3260G>A| |
S153 S213 |
| 177011 | BAA02g18650 | A02 | 9553319 | G | A | downstream_gene_variant | MODIFIER | c.*3367G>A| |
S149 |
| 177012 | BAA02g18650 | A02 | 9554220 | C | T | downstream_gene_variant | MODIFIER | c.*4268C>T| |
S255 |
| 177013 | BAA02g18650 | A02 | 9554350 | G | A | downstream_gene_variant | MODIFIER | c.*4398G>A| |
S34 |
| 177014 | BAA02g18650 | A02 | 9554529 | G | A | downstream_gene_variant | MODIFIER | c.*4577G>A| |
S278 |
| 177015 | BAA02g18660 | A02 | 9554813 | G | A | splice_region_variant&synonymous_variant | LOW | c.309C>T|p.His103His |
S116 |
| 177016 | BAA02g18660 | A02 | 9555223 | T | G | intron_variant | MODIFIER | c.171+17A>C| |
S186 |
| 177017 | BAA02g18660 | A02 | 9555256 | C | T | missense_variant | MODERATE | c.155G>A|p.Arg52Lys |
S105 S106 |
| 177018 | BAA02g18660 | A02 | 9555905 | C | T | upstream_gene_variant | MODIFIER | c.-495G>A| |
S124 |
| 177019 | BAA02g18660 | A02 | 9556731 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S74 |
| 177020 | BAA02g18660 | A02 | 9556789 | G | A | upstream_gene_variant | MODIFIER | c.-1379C>T| |
S223 |
| 177021 | BAA02g18660 | A02 | 9557594 | T | C | upstream_gene_variant | MODIFIER | c.-2184A>G| |
S239 |
| 177022 | BAA02g18660 | A02 | 9558059 | C | T | upstream_gene_variant | MODIFIER | c.-2649G>A| |
S249 |
| 177023 | BAA02g18660 | A02 | 9558133 | C | T | upstream_gene_variant | MODIFIER | c.-2723G>A| |
S69 |
| 177024 | BAA02g18660 | A02 | 9558192 | G | A | upstream_gene_variant | MODIFIER | c.-2782C>T| |
S28 |
| 177025 | BAA02g18660 | A02 | 9558384 | G | A | upstream_gene_variant | MODIFIER | c.-2974C>T| |
S184 |